How do you diagnose dementia and assess its severity?

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Diagnosing Dementia and Assessing Its Severity

Dementia diagnosis requires a multi-dimensional assessment approach that combines patient history, cognitive testing, functional evaluation, and informant reports, with diagnosis based on cognitive or behavioral symptoms that interfere with daily functioning, represent a decline from previous levels, and are not explained by delirium or psychiatric disorders. 1

Core Diagnostic Criteria for Dementia

  • Dementia is diagnosed when cognitive or behavioral symptoms:

    • Interfere with ability to function at work or usual activities 1
    • Represent a decline from previous functioning 1
    • Are not explained by delirium or major psychiatric disorder 1
    • Are detected through history-taking and objective cognitive assessment 1
  • Key cognitive domains to assess include:

    • Memory (impaired ability to acquire and remember new information) 1
    • Executive function (impaired reasoning, judgment, and handling of complex tasks) 1
    • Visuospatial abilities (inability to recognize faces or objects despite good acuity) 1
    • Language functions (difficulty with speaking, reading, writing) 1
    • Personality and behavior changes (mood fluctuations, apathy, social withdrawal) 1

Diagnostic Assessment Tools

Cognitive Screening Tests

  • Initial cognitive screening tools:

    • Mini-Mental State Examination (MMSE) - widely used with high sensitivity and specificity for moderate dementia 1, 2
    • Montreal Cognitive Assessment (MoCA) - more sensitive for mild cognitive impairment and early dementia 1, 2
    • Mini-Cog test - comparable performance to MMSE with good sensitivity (0.91) and specificity (0.86) 2
    • Clock Drawing Test - useful supplementary test 1
  • For atypical presentations:

    • Dementia Cognitive Questionnaire (DCQ) - specifically developed for atypical syndromes like frontotemporal dementia 1
    • Addenbrooke's Cognitive Examination-Revised (ACE-R) - high sensitivity (0.92) and specificity (0.89) 2
  • Important caveat: Diagnosis should not be solely based on impaired cognitive screening test results 1

Functional Assessment

  • Evaluate impact on Activities of Daily Living (ADLs) and Instrumental Activities of Daily Living (IADLs) using:
    • Disability Assessment in Dementia (DAD) 1
    • Functional Activities Questionnaire (FAQ) 1
    • Lawton Instrumental Activities of Daily Living Scale 1
    • Functional Assessment Staging Scale (FAST) 1

Behavioral Assessment

  • Evaluate behavioral and psychological symptoms using:
    • Neuropsychiatric Inventory-Questionnaire (NPI-Q) - brief version for clinical practice 1
    • Geriatric Depression Scale (GDS) or Patient Health Questionnaire (PHQ-9) 1
    • Mild Behavioral Impairment Checklist (MBI-C) 1

Informant Reports

  • Obtaining corroborative history is essential and has prognostic significance 1
  • Recommended informant-based tools:
    • Everyday Cognition (ECog) - for cognitive changes 1
    • Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) - for cognitive and functional changes 1
    • Quick Dementia Rating System (QDRS) - for cognitive and functional changes 1

Diagnostic Workup

Laboratory Testing

  • Standard dementia medical workup should include:
    • Thyroid-stimulating hormone (TSH) 3, 4
    • Vitamin B12 levels 3, 4
    • Other tests guided by history and physical examination 4

Neuroimaging

  • Anatomical neuroimaging is recommended in most situations, especially with:

    • Onset of cognitive symptoms within past 2 years 1
    • Unexpected decline in cognition/function 1
    • Recent significant head trauma 1
    • Unexplained neurological manifestations 1
    • Significant vascular risk factors 1
  • MRI is preferred over CT, especially for detecting vascular lesions 1

    • Recommended sequences: 3D T1 volumetric, FLAIR, T2, and diffusion-weighted imaging 1

Assessing Severity of Dementia

  • Severity assessment should be based on:

    • Degree of cognitive impairment (using standardized tests like MMSE or MoCA) 1
    • Level of functional impairment in daily activities 1
    • Presence and severity of behavioral symptoms 1
  • For longitudinal tracking:

    • MMSE is recommended as a primary tool for tracking cognitive changes over time 1
    • Assessment should occur every 6-12 months, with more frequent assessment for patients with behavioral symptoms 1
    • Use longitudinal serial cognitive assessments (like QuoCo curves) to optimize accuracy 1

Special Considerations

Subjective Cognitive Decline (SCD)

  • For patients with cognitive concerns but normal testing:
    • Conduct appropriate diagnostic workup to identify reversible causes 1
    • Obtain reliable informant information about changes in cognition, function, and behavior 1
    • Use structured scales for objective and subjective cognition 1
    • For negative corroborative history: provide reassurance and follow-up as needed 1
    • For positive corroborative history: schedule annual follow-ups 1

Mild Cognitive Impairment (MCI)

  • Differentiation from dementia rests on whether there is significant interference with daily functioning 1
  • Montreal Cognitive Assessment (MoCA) has the best performance for detecting MCI with 0.89 sensitivity and 0.75 specificity 2

Tracking Response to Treatment and Disease Progression

  • Use a multi-dimensional approach that includes assessment of:

    • Cognition (using MMSE, MoCA, or other validated tools) 1
    • Functional autonomy (using DAD, FAQ, or other functional scales) 1
    • Behavioral symptoms (using NPI-Q or other behavioral scales) 1
    • Caregiver burden (using Zarit Burden Interview) 1
  • All domains must be evaluated at least annually, with more frequent assessment for patients with behavioral symptoms 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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